ライフサイエンスコーパス: cineole

1 a series of terpene molecules, including 1,8-cineole.

2 ization reaction from alpha-terpineol to 1,8-cineole.

3 d (E)-beta-ocimene, and it does not form 1,8-cineole.

4 edione, and acetone, or the monoterpene, 1,8-cineole.

5 The main compounds of the REO were 1.8 cineole (52.2%), camphor (15.2%) and alpha-pinene (12.4%

6 s roots resulted in the rapid release of 1,8-cineole, a monoterpene that has not been previously repo

7 clade catalyzes the formation of mostly 1,8-cineole; a sesquiterpene synthase belonging to the TPS-a

8 Both 1,8-cineole and d-camphor are C(10) monoterpenes containing

9 bition caused by the natural monoterpene 1,4-cineole and its structurally related herbicide cinmethyl

10 enal was the most intense odorant, while 1,8-cineole and linalool were also revealed as important aro

11 N. obtusifolia emitted solely 1,8-cineole and no monoterpenes were found in floral scents

12 nthases produce (+)-bornyl diphosphate, 1, 8-cineole, and (+)-sabinene, respectively, as their major

13 yses identified linalool, hexyl acetate, 1,8-cineole, and butyl acetate as key aroma compounds of thi

14 ular monoterpenes, for example linalool, 1,8-cineole, and camphor.

15 on of plant tissue, the recent report of 1,8-cineole as an Arabidopsis root volatile suggests that th

16 n of cineole, enabling C. braakii to live on cineole as its sole source of carbon and energy.

17 tic 'cineole cassette' monoterpenes with 1,8-cineole as the dominant volatile product.

18 cation of the hyp3 gene, responsible for 1,8-cineole biosynthesis, the first monoterpene synthase dis

19 Cells were stimulated with the odour cineole by rapid exchange of the solution bathing the ol

20 es emit a characteristic blend including the cineole cassette monoterpenes.

21 A monoterpene synthase producing the set of 'cineole cassette' compounds was isolated from N. noctifl

22 To determine the origin of the 'cineole cassette' monoterpene phenotype other potential

23 characteristic floral scent comprising the' cineole cassette' monoterpenes 1,8-cineole, limonene, my

24 ynthesize simultaneously the characteristic 'cineole cassette' monoterpenes with 1,8-cineole as the d

25 All previously isolated 'cineole cassette'-monoterpene synthase genes are multi p

26 that synthesize the seven compounds of the 'cineole cassette'.

27 ent increased more gradually with increasing cineole concentration and did not saturate within the 10

28 id not saturate within the 100-fold range of cineole concentrations applied.When stimulated for 30 s

29 The LiCINS mRNA levels paralleled the 1,8-cineole content in mature flowers of the three lavender

30 atalytic mechanism of alpha-terpineol-to-1,8-cineole conversion is initiated by a catalytic dyad (his

31 This initiates the biodegradation of cineole, enabling C. braakii to live on cineole as its s

32 n the samples occurred in the amounts of 1,8-cineole, fenchone and trans-alpha-necrodyl acetate.

33 that produce terpene molecules, such as 1,8-cineole, have been little explored in fungi, providing a

34 scence indicating that the production of 1,8 cineole in Lavandula is most likely controlled through t

35 tae, are rich in monoterpenes, including 1,8-cineole, limonene, beta-myrcene, alpha- and beta-pinene,

36 sing the' cineole cassette' monoterpenes 1,8-cineole, limonene, myrcene, beta-pinene, alpha-pinene, s

37 ies to Arabidopsis roots did not produce 1,8-cineole nor any C6 wound-VOCs; compatible interactions b

38 zed by multiproduct enzymes, with either 1,8-cineole or alpha-terpineol contributing most to the vola

39 The presence of either 1,4-cineole or cinmethylin stimulated root uptake of [(14)C]

40 to the volatile spectrum, thus referring to cineole or terpineol synthase, respectively.

41 Cells were exposed to the odour cineole or to solutions of modified ionic content by rap

42 ns, including members of the p-menthane (1,8-cineole), pinane (alpha- and beta-pinene), thujane (isot

43 oterpenes from geranyl diphosphate, with 1,8-cineole predominating.

44 2)O, 2,2,5,5-tetramethyltetrahydrofuran, and cineole proceed via dimer-based transition structures [(

45 Through genome sequencing of cineole-producing isolate E7406B, we were able to identi

46 d 266 that determine the different terpineol-cineole ratios in Nicotiana suaveolens cineole synthase

47 is of the putative metabolite, 2-hydroxy-1,4-cineole, showed that the cis-enantiomer was much more ac

48 hemical formation of alpha-terpineol and 1,8-cineole, site-directed mutagenesis, in silico modeling,

49 rized cDNA with strong homology to known 1,8-cineole synthase (CINS) genes.

50 ineol-cineole ratios in Nicotiana suaveolens cineole synthase and Nicotiana langsdorffii terpineol sy

51 nthase genes of e.g. N. alata rather than to cineole synthase genes of e.g. N. forgetiana.

52 The 1,8-cineole synthase produces significant amounts of (+)- an

53 ation-cyclization mechanism of action of 1,8-cineole synthase.

54 ee construction clustered the newly isolated cineole synthases (CIN) of section Alatae together with

55 cal for water capture and specificity during cineole synthesis, the same mechanism used in an unrelat

56 ible for aroma perception were limonene, 1,8-cineole, terpinen-4-ol, estragole and trans-anethole, an

57 braakii that catalyzes the hydroxylation of cineole to (S)-6beta-hydroxycineole.

58 P450cin catalyzes the monooxygenation of 1,8-cineole, which is structurally very similar to d-camphor

59 near monoterpene precursor) primarily to 1,8-cineole with K ( m ) and k ( cat ) values of 5.75 muM an